BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    QUANTA LITE B2 GPI SCREEN

    FDA 510(k)
    FDA Class 2 ·Immunology

    Medtronic Reusable Instruments

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00721902575549·INSTRUMENT 8980230 TWO PRONG TIP 30MM

    247

    FDA UDI
    SUNTECH MEDICAL, INC.·10840935106562·

    NEB-U-MASK SYSTEM, MODELS 1895, 1896

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NEST Interbody System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OLMPUS VIDEO TELESCOPES

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FBP·February 1, 2013

    HEARTSTART ONSITE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·July 2, 2014

    HEARTMATE II LEFT VENTRICULAR ASSIST DEVICE

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·February 1, 2011

    M2A-MAGNUM PF CUP 56OD/50ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·August 25, 2016

    M2A-MAGNUM MOD HD SZ 50MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·August 25, 2016

    M2A 38MM MOD HD STD NK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·April 24, 2018